Endovenous device for dispersing a dilating agent

ABSTRACT

Apparatus and methods are disclosed for inserting electrical leads within a heart. A method is provided for positioning a medical electrical lead in a cardiac vein. The method comprises inserting a lead within a coronary sinus, dispersing at least one vasodilating agent to dilate at least one cardiac vein, and inserting the lead into a dilated cardiac vein.

This application is a Divisional of application Ser. No. 10/041,802,filed Oct. 29, 2001, entitled “Method and Apparatus for EndovenousPacing Lead,” now U.S. Pat. No. 6,936,040.

FIELD OF THE INVENTION

This invention relates generally to a method and apparatus forelectrically stimulating a heart, and, more particularly, to a methodand apparatus for positioning and fixating an electrode lead tostimulate and/or sense activity in the heart.

DESCRIPTION OF THE RELATED ART

Since their earliest inception some forty years ago, there has been asignificant advancement in body-implantable electronic medical devices.Today, these implantable devices include therapeutic and diagnosticdevices, such as pacemakers, cardioverters, defibrillators, neuralstimulators, drug administering devices, among others for alleviatingthe adverse effects of various health ailments. Today's implantablemedical devices are also vastly more sophisticated and complex thantheir predecessors, and are therefore capable of performing considerablymore complex tasks for reducing the effects of these health ailments.

A variety of different implantable medical devices (IMD) are availablefor therapeutic stimulation of the heart and are well known in the art.For example, implantable cardioverter-defibrillators (ICDs) are used totreat patients suffering from ventricular fibrillation, a chaotic heartrhythm that can quickly result in death if not corrected. In operation,the ICD continuously monitors the electrical activity of a patient'sheart, detects ventricular fibrillation, and in response to thatdetection, delivers appropriate shocks to restore normal heart rhythm.Similarly, an automatic implantable defibrillator (AID) is available fortherapeutic stimulation of the heart. In operation, an AID devicedetects ventricular fibrillation and delivers a non-synchronoushigh-voltage pulse to the heart through widely spaced electrodes locatedoutside of the heart, thus mimicking transthoratic defibrillation. Yetanother example of a prior art cardioverter includes thepacemaker/cardioverter/defibrillator (PCD) disclosed, for example, inU.S. Pat. No. 4,375,817 to Engle, et al. This device detects the onsetof tachyarrhythmia and includes means to monitor or detect progressionof the tachyarrhythmia so that progressively greater energy levels maybe applied to the heart to interrupt a ventricular tachycardia orfibrillation. Numerous other, similar implantable medical devices, forexample a programmable pacemaker, are further available.

Regardless of the exact construction and use, each of theabove-described IMDs generally comprise three primary components: alow-power control circuit, a high-power output circuit, and a powersource. The control circuit monitors and determines various operatingcharacteristics, such as, for example, rate, synchronization, pulsewidth and output voltage of heart stimulating pulses, as well asdiagnostic functions such as monitoring the heart. Conversely, thehigh-power output circuit generates electrical stimulating pulses to beapplied to the heart via one or more leads in response to signals fromthe control circuit.

The power source “powers” both the low-power control circuit and thehigh-power output circuit. As a point of reference, the power source istypically required to provide 10-20 microamps to the control circuit anda high power pulse to the output circuit. Depending upon the particularIMD application, the high-power output circuit may require a stimulationenergy of as little as 0.1 Joules for pacemakers to as much as 40 Joulesfor implantable defibrillators. In addition to providing sufficientstimulation energy, the power source must possess a low self-dischargeto have a useful life of many years, must be highly reliable, and mustbe able to supply energy from a minimum packaged volume.

Modern electrical therapeutic and diagnostic devices for the heartrequire a reliable electrical connection between the device and aparticular region of the heart. Typically, a medical electrical “lead”is used for the desired electrical connection. One type of commonly usedimplantable lead is a transvenous lead. Transvenous leads are positionedthrough the venous system to attach or electrically connect at theirdistal end to the heart. At their proximal end, they are typicallyconnected to the electrical therapeutic and diagnostic device, which maybe implanted. Such leads normally take the form of a long, generallystraight, flexible, insulated conductor. Among the many advantages oftransvenous leads is that they permit an electrical contact with theheart without physically exposing the heart itself, i.e., major thoracicsurgery is not required.

The specific design of transvenous leads is varied, depending upon theregion of the heart to which it is to be connected. For example, U.S.Pat. No. 6,070,104 discloses an implantable lead capable of stimulatingand/or sensing multiple chambers of the heart. Multiple electrodes arelocated on the lead and spaced apart so that multiple chambers may beseparately stimulated and/or sensed. The structure and size of patients'hearts varies considerably. Accordingly, the optimal locations forpositioning the electrodes within a vein may vary substantially,depending on the anatomy of the patient.

The left ventricle is a portion of the heart that can be difficult inwhich to locate a lead due to the specific anatomical structure of theheart. One type of implantable lead that is used for positioningadjacent to the left ventricle is an endovenous epicardial lead. Atypical left ventricular endovenous epicardial lead is one that isinitially routed in the typical manner into the right atrium of theheart. From the right atrium the lead is guided through the coronarysinus and into a cardiac vein that is attached to the left side of theheart. The lead is then inserted into the cardiac vein and extended inan attempt to reach a desired distal location adjacent to the leftventricle of the heart. This procedure is difficult due to the tortuouspath that the lead is subjected to and due to the reduced diameter ofthe cardiac veins in the more distal locations. Another factor thatcomplicates the left ventricular procedure is that the leads are limitedin active fixation mechanisms. Right ventricular leads can utilizefixation mechanisms such as tines and screw-in lead tips. These fixationmethods may be difficult for use with left ventricular leads due to thespecific anatomical structure of the left sided endovenous system.

There is a need for improved methods and apparatus for more efficientplacement and fixation of endovenous epicardial left ventricular pacingleads within a heart.

SUMMARY OF THE INVENTION

In one aspect of the present invention, an apparatus is provided forpositioning a medical electrical lead in a heart. The medical electricallead comprises an electrode coupled adjacent a distal end portion of themedical electrical lead, the distal end portion of the lead capable ofinsertion into the coronary sinus of a patient. A distribution device isattached to the distal end of the lead and adapted for dissipation of amaterial into the coronary sinus and into a cardiac vein. The materialcan comprise a vasodilating agent.

In another embodiment of the invention a medical catheter devicecomprising a flexible tubular body having a distal end and a proximalend is disclosed. A first lumen is disposed within the flexible tubularbody and is capable of transporting an electrical lead through the firstlumen and out the distal end of the flexible tubular body. There is alsoa distribution device capable of emitting a vasodilating agent adjacentthe distal end of the flexible tubular body.

In yet another aspect of the present invention, a method for positioninga medical electrical lead in a cardiac vein is disclosed. The methodcomprises inserting a lead within a portion of a patient's body,dispersing at least one vasodilating agent to dilate at least onevessel, and inserting the lead into a dilated vessel.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention may be understood by reference to the followingdescription taken in conjunction with the accompanying drawings, inwhich like reference numerals identify like elements, and in which:

FIG. 1 schematically illustrates a prior art embodiment of an implantedmedical device with an associated lead positioned within the rightventricle of a heart;

FIG. 2 schematically illustrates a prior art embodiment of an implantedmedical device with an endovenous epicardial lead positioned adjacentthe left ventricle of a heart;

FIG. 3 is a perspective view of a guide catheter constructed inaccordance with the principles of the present invention;

FIG. 4 illustrates an alternative distal end of the guide catheter ofFIG. 3, designed specifically for introduction to the coronary sinus;

FIG. 5A schematically illustrates an alternate embodiment guide catheterconstructed in accordance with the principles of the present invention;

FIG. 5B schematically illustrates the alternate embodiment guidecatheter shown in FIG. 5A dispersing vasodilating agents into a cardiacvein in accordance with the principles of the present invention;

FIG. 6 schematically illustrates an alternate embodiment guide catheterconstructed in accordance with the principles of the present invention;

FIG. 7 schematically illustrates an alternate embodiment guide catheterconstructed in accordance with the principles of the present invention;

FIG. 8 schematically illustrates an alternate embodiment guide catheterconstructed in accordance with the principles of the present invention;

FIG. 9 shows cross-sectional views of one embodiment of the invention;and

FIG. 10 illustrates cross-sectional views of one particular embodimentof the invention.

While the invention is susceptible to various modifications andalternative forms, specific embodiments thereof have been shown by wayof example in the drawings and are herein described in detail. It shouldbe understood, however, that the description herein of specificembodiments is not intended to limit the invention to the particularforms disclosed, but, on the contrary, the intention is to cover allmodifications, equivalents, and alternatives falling within the scope ofthe invention as defined by the appended claims.

DETAILED DESCRIPTION OF SPECIFIC EMBODIMENTS

Illustrative embodiments of the invention are described below. In theinterest of clarity, not all features of an actual implementation aredescribed in this specification. It will of course be appreciated thatin the development of any such actual embodiment, numerousimplementation-specific decisions must be made to achieve thedevelopers' specific goals, such as compliance with system-related andbusiness-related constraints, which will vary from one implementation toanother. Moreover, it will be appreciated that such a development effortmight be complex and time-consuming, but would nevertheless be a routineundertaking for those of ordinary skill in the art having the benefit ofthis disclosure.

Embodiments of the present invention concern an electrical lead that maybe implanted and used to stimulate and/or sense the atrium and ventricleof the left side of the heart through the coronary sinus. As is wellknown, there has to date been a great difficulty in reliably implantingleads within the coronary sinus and cardiac veins. For example, atypical coronary sinus is 10 millimeters at its largest diameter (nearthe outflow to the right atrium) and narrows until it has a diameter ofbetween approximately 2-3 millimeters and merges to the great cardiacvein. Thus any leads having larger sizes could be expected to diminishthe flow of blood through the coronary sinus. The fixation of a leadwithin the coronary sinus or cardiac vein is further complicated by thefact that, unlike a heart chamber where the fibrotic tissue response isused to assist lead fixation, no such fibrotic response can be expectedin the vein. As such no fibrotic tissue response is available to assistin lead fixation. Thus, embodiments of the present invention comprise alead implantation apparatus and method that includes the dispensing of avasodilating agent that induces a temporary dilating of the venousvessels during positioning of the lead. The vasodilating agent generallyrelaxes the cardiac vein, thereby making it easier to insert the cardiaclead into more distal locations. Once the effects of the vasodilatingagent has ceased, the cardiac vein will contract to its original size,thus fixating the cardiac lead by the contraction produced by thevascular musculature. This fixation can enable an increased leadstability and thereby an increased performance of the lead.

FIG. 1 illustrates a prior art implantable medical device (IMD) system10, which includes an implantable electronic device 12, such as apacemaker, defibrillator, or the like, that has been implanted in apatient. The device 12 is housed within a hermetically sealed,biologically inert outer canister or housing, which may itself beconductive so as to serve as an electrode in the pacemaker'spacing/sensing circuit. One or more pacemaker leads, collectivelyidentified with reference numeral 14 in FIG. 1 are electrically coupledto the pacemaker 12 in a conventional manner and extend into thepatient's heart 16 via a vein, typically the superior vena cava vein 18.

Disposed generally near a distal end 20 of the leads 14 are one or moreexposed conductive electrodes for sensing cardiac activity, deliveringelectrical pacing stimuli to the heart 16, or providing a stimulatingvoltage to defibrillate the heart 16. The leads 14 may be implanted withtheir distal end situated adjacent the right atrium 22 or the rightventricle 24, or both, of the heart 16. The illustration of FIG. 1 showsthe distal end 20 of the lead 14 disposed within the right ventricle 24of the heart 16. Due to the anatomical structure of the heart 16, it ismore difficult to position a lead 14 within or adjacent to the leftatrium 26 or left ventricle 28. The septum 30 is a wall that separatesthe right cavities 22, 24 from the left cavities 26, 28 of the heart 16and prevents direct fluid communication between them. The septum 30likewise presents a barrier to direct insertion of the lead 14 intoeither of the left cavities 26, 28 using the typical pathway of thesuperior vena cava 18. An alternate path to a location adjacent the leftcavities 26, 28 is through the coronary sinus 32 that provides apassageway for oxygen depleted blood from the left side of the heart 16to enter the right atrium 22.

FIG. 2 schematically illustrates a prior art embodiment of an implantedmedical device with an endovenous epicardial lead 14 passing through thesuperior vena cava 18, through the right atrium 22, entering thecoronary sinus 32 and its distal end 20 positioned within a cardiac vein34 adjacent to the left ventricle 28 of a heart 16. The ability toposition a lead 14 within this section of the heart 16 enables theimplantable medical device (IMD) system 10 to provide left ventricle 28and atrial 26 pacing, coronary sinus 32 defibrillation, left ventricle28 defibrillation, other delivery of therapy and/or other form ofsensing.

As discussed above, the placement of a lead 14 within the coronary sinus32 and into a cardiac vein 34 may be problematic due to the physicalrestrictions and the difficulty in fixating the distal end 20 of thelead 14. The various embodiments of the present invention address theseissues and are described herein. To the extent that certain componentsand procedures referenced herein are conventional in their design andoperation, such components/procedures will not be described herein indetail, as it is believed that design and implementation of suchcomponents and the performance of such methods would be a matter ofroutine practice to those of ordinary skill in the art. For example,various processes for passing a catheter lead through the tortuous pathof a representative cardiac venous system is well known in the art.

Referring now to FIG. 3, an exemplary guide catheter 40 includes aflexible tubular body 42 having a distal end 44 and a proximal end 46. Adistributor 48 is mounted on the distal end 44 of the flexible tubularbody 42, and a hub 50 is mounted on the proximal end 46 of the flexibletubular body 42. The axial lumen 52 of the tubular body 42 provides apassageway for a lead (e.g., an electrical lead) to be directed out ofthe distal end 44 of the catheter 40. A secondary connector 54 isconnected to the tubular body 42 and to a secondary passageway or lumen56 that is connected to the distributor 48. The secondary connector 54,second lumen 56, and the distributor 48 provide a means for transportinga material from the proximal end 46 to the distal end 44 of the catheter40. The distributor 48 provides a means of dispersing the materialwithin a vessel, such as a coronary sinus and/or a cardiac vein. Thematerial can comprise a vasodilating agent that promotes the dilation ofthe one or more vessels which the vasodilating agent contacts. Examplesof vasodilating agents that can be used include Papaverin and Moxaverin.

The dispensing of the vasodilating agent induces a temporary dilating ofthe venous vessels, relaxing the cardiac veins, thereby making it easierto place a cardiac lead through the axial lumen 52 of the catheter 40and into more distal locations in the vessel, such as a cardiac vein.After placement of the lead within the vessel, the catheter 40 can beremoved, while leaving the lead implanted within the vessel. Once theeffects of the vasodilating agent has ceased, the vessel will generallycontract to its original size, thus assisting the fixation of the leadwithin the vessel. Thus the vasodilating agent can assist in theplacement of the lead into more distal locations within the heart andcan assist in the fixation of the lead within the vessel once placed.This fixation can provide increased lead stability and thereby anincreased performance of the lead. It is possible that the secondaryconnector 54 can connect directly to the axial lumen 52 rather than aseparate passageway 56 as shown. Vasodilating agents can be injectedthrough the secondary connector 54, through the axial lumen 52 and tothe distal end 44 of the catheter 40 for distribution either through thedistributor 48 or out the end of the catheter 40.

FIG. 4 illustrates an alternate distal end 44 of the tubular body 42 ofthe catheter 40 embodiment shown in FIG. 3. This illustration isconfigured for introduction of the distal end 44 of the tubular body 42into the coronary sinus.

Referring to FIG. 5A, an exemplary guide catheter 60 is shown insertedinto the superior vena cava 18, passing through the right atrium 22 andpassing into the coronary sinus 32. The guide catheter 60 comprises aflexible tubular body 62 having a distal end 64 and a proximal end 66.At the distal end 64 of the tubular body 62 is a distributor 68, whichis shown within the guide catheter 60. An alternate passageway 70provides a path from the proximal end 66 of the catheter 60 to thedistributor 68 at the distal end 64 of the tubular body 62.

FIG. 5B shows the guide catheter 60 inserted through the coronary sinus32 to the cardiac veins 34. A vasodilating agent 72 is shown dispensedfrom the distributor 68 at the distal end 64 of the catheter 60. Inresponse to pressure applied by an injector element 71, the vasodilatingagent 72 is forced through the alternate passageway 70 and is dispersedfrom the distributor 68 into one or more of the cardiac veins 34,promoting dilation of the cardiac veins 34. Upon the dilation of thecardiac veins 34 it may be possible to insert the guide catheter 60further into one of the cardiac veins 34, where a lead can be disposedinto a more distal location within the cardiac vein than would bepossible without the dilating effects promoted by the vasodilating agent72. An alternate procedure entails the dispensing of the vasodilatingagent 72 out the distal end 64 of the catheter 60, followed by theinsertion of an electrical lead (not shown) through the catheter 60, outthe distal end 64 and into one of the cardiac veins 34 that are dilatedfrom the effects of the vasodilating agent 72.

FIG. 6 presents an alternate embodiment of a catheter device 40 a havinga flexible tubular body 42 and a distribution device 48 locatedapproximate the distal end 44 of the device 40 a. A secondary passageway56 connects to the distribution device 48 and enables vasodilatingagents to be transported to the distribution device 48. The distributiondevice 48 may comprise a porous material that dissipates thevasodilating agents in a substantially controlled manner. Thedistribution device 48 can typically dispense the vasodilating agents ina more uniform pattern than dispensing without the use of a distributiondevice 48.

FIG. 7 presents an alternate embodiment of a catheter device 40 b havinga flexible tubular body 42 and a distribution device 48 locatedapproximate the distal end 44 of the device 40 b. In this particularembodiment there is no separate passageway for transmitting thevasodilating agents to the distribution device 48. The distributiondevice 48 can be impregnated with the vasodilating agents prior to thecatheter device 40 b being inserted into the patient. The designparameters of the distribution device 48 material, such as porosity ofthe material and the relative surface tensions of the distributiondevice 48 material and the vasodilating agents, will determine the rateof dissipation of the vasodilating agents from the distribution device48. The distribution device 48 can comprise a sponge-like substance thatcan be saturated or impregnated by the vasodilating agents. Vasodilatorscan also be applied by chemically binding to or modifying thedistribution device 48 material.

Cardiac pacing leads can also be inserted and placed within a patientwithout the use of a catheter device. In these cases the vasodilatoragents can be applied through the cardiac pacing lead itself. Cardiacpacing leads can comprise an elongated flexible body. The body of thelead can have a tubular shape and can be constructed of polyurethane orother similar material used within the medical industry for use insidethe human body. The lead can comprise a core of electrically conductivematerial that is surrounded by a layer of insulative material. The leadwill typically include an electrode that is coupled to or adjacent tothe distal end of the lead. The lead can include an expandable helicalcoil coupled to its distal end.

FIG. 8 presents an alternate embodiment of the invention comprising anelectrical lead device 40 c having an elongated flexible tubular body 42and a distal end 44. In this particular embodiment the tubular body 42comprises a first section 74 and a more distal second section 76 thathas a smaller diameter than the first section 74. The lead 40 c can betapered along a longitudinal axis of the elongated flexible body 42. Thetapered shape can assist in the placement of the lead 40 c to moredistal locations within a vessel, such as a cardiac vein. The firstsection 74 has distribution apertures 75 and the second section 76 hasdistribution apertures 77, both capable of dispersing a vasodilatingagent. There can be separate passageways to each of the first and secondsection apertures 75, 77, which enable the dispersion of differentquantities of vasodilating agents from each.

The reduced diameter of the second section 74 can enable the insertionof the electrical lead device 40 c into more distal locations within thepatient. The particular embodiment shows protrusions 78 from the distalend 44 of the lead 40 c. The protrusions 78 can assist in providingelectrical contact between the lead 40 c and the cardiac vein and canassist in the fixation mechanism of the lead 40 c to the heart.Anchoring means attached to the distal end 44 of the lead 40 c canassist the fixation of the lead within a cardiac vein. Examples ofanchoring means include projections, expanding helical coils and ribs onthe exterior surface of the lead. These can all assist with thecontraction of the vein in providing a fixation of the lead within thecardiac vein.

In some cases a guide wire is used to initiate the insertion into aparticular location within the heart, such as a cardiac vein. The guidewire can be used in conjunction with the lead, such as having the guidewire proceed through a axial lumen within the lead, whereby after theplacement of the lead the guide wire can be removed from the lumen,leaving the lead implanted within the patient. These leads are commonlyreferred to as an “over-the-wire” type of implantable electrical lead.

FIG. 9 shows cross-sectional views of one embodiment of the inventioncomprising a pacing lead 80 a having a first lumen 82 and a second lumen84. The first lumen 82 is used to house a guide wire 86 while the secondlumen 84 provides a passageway to the distal end 88 of the lead 80 a.The second lumen 84 can be used to transport and dispense vasodilatingagents to the distal end 88 of the lead 80 and can comprise a pluralityof outlets 90 to dissipate the vasodilating agents.

FIG. 10 illustrates cross-sectional views of one particular embodimentof the invention in which the vasodilating agents are transferred to thedistal end of the lead through the annulus area between the guide wireand the lumen within the lead. The embodiment of FIG. 10 comprises apacing lead 80 b having a first lumen 82 used to house a guide wire 86.An annulus area 92 between the first lumen 82 and the guide wire 86 canbe used to transport and dispense vasodilating agents to the distal end88 of the lead 80 b and can comprise a plurality of outlets 94 along thelength of the lead 80 to dissipate the vasodilating agents. As with theembodiments of catheter devices, such as shown in FIG. 6, the embodimentof the lead 80 shown in FIG. 10 can further comprise a means ofdistribution to more evenly dissipate the vasodilating agent (e.g. adistribution device 48).

The particular embodiments disclosed above are illustrative only, as theinvention may be modified and practiced in different but equivalentmanners apparent to those skilled in the art having the benefit of theteachings herein. Furthermore, no limitations are intended to thedetails of construction or design herein shown, other than as describedin the claims below. It is therefore evident that the particularembodiments disclosed above may be altered or modified and all suchvariations are considered within the scope of the invention.Accordingly, the protection sought herein is as set forth in the claimsbelow.

1. A medical electrical lead device, comprising: an elongated flexiblelead body having a distal end portion and a proximal end portion, thelead body being adapted for insertion through a superior vena cava of apatient and passage through a coronary sinus of a patient to positionthe distal end within a cardiac vein adjacent to a left ventricle of apatient; an electrode coupled to the distal end of the lead body; meanscoupled to the distal end of the lead body for anchoring the electrodewithin the cardiac vein; and means formed at the distal end portion ofthe lead body proximal to the electrode for dispersing a vasodilatingagent within a vessel during insertion and passage of the lead body toposition the distal end within the cardiac vein, wherein thevasodilating agent is delivered along the lead body to the means fordispersing from the proximal end, and wherein the means for dispersingincludes a plurality of apertures formed in the lead body to dispersethe vasodilating agent.
 2. A medical electrical lead device as set forthin claim 1, wherein the lead is an over-the-wire lead.
 3. A medicalelectrical lead device, as set forth in claim 1, wherein the elongatedflexible body comprises a flexible tube, and the apertures are formed inthe flexible tube.
 4. A medical electrical lead device, as set forth inclaim 1, wherein the elongated flexible body comprises a tubeconstructed with material selected from the group consisting ofpolyurethane and silicone.
 5. A medical electrical lead device, as setforth in claim 1, wherein said lead is tapered along a longitudinal axisof the elongated flexible body.
 6. A medical electrical lead device, asset forth in claim 1, wherein the lead comprises a core of electricallyconductive material surrounded by a layer of insulative material.
 7. Amedical electrical lead device as set forth in claim 1, wherein theanchoring means comprises an expandable helical coil coupled to itsdistal end.
 8. The medical electrical lead device of claim 1, furthercomprising a fluid source containing the vasodilating agent, wherein thesource is coupled to provide the vasodilating agent to the dispersingmeans.
 9. The medical electrical lead device of claim 1, furthercomprising: a first lumen to accommodate a guide wire; and a secondlumen that receives the vasodilating agent at the proximal end of thesecond lumen and delivers the vasodilating agent along the lead body tothe means for dispersing, wherein the second lumen defines the pluralityof apertures.
 10. The medical electrical lead device of claim 1, furthercomprising a lumen to accommodate a guide wire, receive the vasodilatingagent at the proximal end of the lumen, and deliver the vasodilatingagent along the lead body to the means for dispersing in an annulus areabetween the guide wire and the lumen, wherein the lumen defines theplurality of apertures.
 11. The medical electrical lead device of claim1, wherein the plurality of apertures are formed at different positionsalong a length of the elongated flexible lead body, and some of theapertures are configured to disperse different quantities of thevasodilating agent.
 12. A medical catheter device, comprising: aflexible tubular body having a distal end and a proximal end; a firstlumen disposed within the flexible tubular body capable of transportingan electrical lead through the first lumen and out the distal end of theflexible tubular body to an implant site within a cardiac vein adjacentto a left ventricle of a patient; means for dispersing a vasodilatingagent within a vessel during insertion and passage of the tubular bodyto position the distal end within the cardiac vein, wherein the meansfor dispersing a vasodilating agent is attached near the distal end ofthe tubular body and comprises a sponge-like material, wherein thevasodilating agent is selectively delivered from the proximal end to themeans for dispersing; and a fluid source containing the vasodilatingagent, wherein the source is coupled to provide the vasodilating agentto the dispersing means.
 13. The medical catheter device of claim 12,wherein the sponge-like material is capable of being saturated orimpregnated with the vasodilating agent.
 14. A medical catheter device,comprising: a flexible tubular body having a distal end and a proximalend; a first lumen disposed within the flexible tubular body capable oftransporting an electrical lead through the first lumen and out thedistal end of the flexible tubular body to an implant site within acardiac vein adjacent to a left ventricle of a patient; means fordispersing a vasodilating agent within a vessel during insertion andpassage of the tubular body to position the distal end within thecardiac vein, wherein the means for dispersing a vasodilating agent isattached near the distal end of the tubular body and the vasodilatingagent is selectively delivered from the proximal end to the means fordispersing; a second lumen for transporting the vasodilating agent fromthe proximal end to the distal end of the tubular body; and a fluidsource containing the vasodilating agent, wherein the source is coupledto provide the vasodilating agent to the second lumen.